Continuous Electrochemical Carbon Capture via Redox-Mediated pH Swing─Experimental Performance and Process Modeling

We investigate a continuous electrochemical pH-swing method to capture CO<sub>2</sub> from a gas phase. The electrochemical cell consists of a single cation-exchange membrane (CEM) and a recirculation of a mixture of salt and phenazine-based redox-active molecules. In the absorption compartment, this solution is saturated by CO<sub>2</sub> from a mixed gas phase at high pH. In the electrochemical cell, pH is reduced, and CO<sub>2</sub> is selectively released in a desorption step. We investigate the influence of redox molecule concentration on the charge storage capacity of the solution, as well as the impact of current density and solution recirculation rate on process performance. A theoretical framework, based on a minimal set of assumptions, is established. This framework describes the data very accurately and can be used for system design and optimization. We evaluate the trade-off between energy consumption and CO<sub>2</sub> capture rate and compare with published reports. We report a low energy consumption of 32 kJ/mol of CO<sub>2</sub> at a capture rate of 39 mmol/m<sup>2</sup>/min.

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Publication Details

Journal
The Journal of Physical Chemistry Letters
Published
2025-01-29
DOI
https://doi.org/10.1021/acs.jpclett.4c03111
Citations
4
Primary Topic
Fuel Cells and Related Materials
Type
article
Field-Weighted Citation Impact
2.92

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article

Continuous Electrochemical Carbon Capture via Redox-Mediated pH Swing─Experimental Performance and Process Modeling

H.V.M. Hamelers, S. Porada, Qingdian Shu, P. M. Biesheuvel et al.
4 citations
The Journal of Physical Chemistry Letters
Fuel Cells and Related Materials
2.92
article

Continuous Electrochemical Carbon Capture via Redox-Mediated pH Swing─Experimental Performance and Process Modeling

H.V.M. Hamelers, S. Porada, Qingdian Shu, P. M. Biesheuvel, Piotr Śledzik
article en
4 citations

Abstract

We investigate a continuous electrochemical pH-swing method to capture CO<sub>2</sub> from a gas phase. The electrochemical cell consists of a single cation-exchange membrane (CEM) and a recirculation of a mixture of salt and phenazine-based redox-active molecules. In the absorption compartment, this solution is saturated by CO<sub>2</sub> from a mixed gas phase at high pH. In the electrochemical cell, pH is reduced, and CO<sub>2</sub> is selectively released in a desorption step. We investigate the influence of redox molecule concentration on the charge storage capacity of the solution, as well as the impact of current density and solution recirculation rate on process performance. A theoretical framework, based on a minimal set of assumptions, is established. This framework describes the data very accurately and can be used for system design and optimization. We evaluate the trade-off between energy consumption and CO<sub>2</sub> capture rate and compare with published reports. We report a low energy consumption of 32 kJ/mol of CO<sub>2</sub> at a capture rate of 39 mmol/m<sup>2</sup>/min.

The Journal of Physical Chemistry LettersVol. 16(5)
Wrocław University of Science and Technology (PL), AGH University of Krakow (PL), Wageningen University & Research (NL)
European Commission, Narodowe Centrum Nauki, Narodowym Centrum Nauki, Narodowa Agencja Wymiany Akademickiej, Wetsus
Openalex Percentile: Top 10%
Fuel Cells and Related Materials
2.92
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Continuous Electrochemical Carbon Capture via Redox-Mediated pH Swing─Experimental Performance and Process Modeling — H.V.M. Hamelers, S. Porada, et al. · The Journal of Physical Chemistry Letters (2025) | TGRS Research Map | TGRS